Trichuris suis ova terapija u inflamatornoj bolesti crijeva: meta-analiza.
Medicine
Sažetak istraživanja
Pozadina Poslednjih godina, terapija Trichuris suis ova (TSO) u inflamatornoj bolesti creva (IBD) privukla je veliku pažnju. Međutim, efikasnost i sigurnost TSO terapije još uvijek nisu dobro opisane.
Cilj studije je bio da se izvrši metaanaliza za procjenu efikasnosti TSO terapije kod IBD.
Metode PubMed, Embase, Web of Science, ClinicalTrials.gov i Cochrane Library pretražene su od početka do avgusta 2017. Uključena su samo randomizirana, dvostruko slijepa, placebom kontrolirana ispitivanja (RCT). Stope objedinjene procjene su izvršene meta-analizom i prijavljene prema standardnim Cochrane smjernicama i PRISMA izjavi.
Rezultati U studiji ulceroznog kolitisa (3 RCT, n = 74), indukovane stope kliničke remisije i kliničkog odgovora bile su 10,8% (4/37) i 53,8% (21/39) u TSO grupi, dok su 6,7% (2/30) i 29,0% (9/31all) u grupi P). Dvadeset dva (9/41) procenta pacijenata u TSO grupi iskusilo je najmanje 1 neželjeni događaj u poređenju sa 27,3% (9/33) placeba [relativni odnos (RR) 0,75, 95% interval pouzdanosti (95% CI) 0,17-3,27]. U studiji Crohnove bolesti (3 RCT, n = 538), 40,7% (74/182) pacijenata u TSO grupi postiglo je kliničku remisiju u poređenju sa 42,9% (90/210) placeba (RR 0,95, 95% CI 0,75-1,20); 45,9% (141/307) pacijenata u TSO grupi je ušlo u klinički odgovor u poređenju sa 45,1% (151/335) placeba (RR 1,02, 95% CI 0,86-1,21). Bilo je oskudnih podataka o neželjenim događajima koji su prijavili i TSO i placebo grupu (RR 1,00, 95% CI 0,88-1,13).
Zaključak TSO terapija nije pokazala statističku korist za pacijente sa IBD, pa je sugerisala da kliničari pažljivo razmotre njenu vrijednost prije nego što se uvedu u kliničku praksu. Možda su daljnja istraživanja veće veličine uzorka neophodna zbog prethodnih rezultata sa nedostatkom snage.
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Trichuris suis ova therapy in inflammatory bowel disease: A meta-analysis.
Background In recent years, Trichuris suis ova (TSO) therapy in inflammatory bowel disease (IBD) has attracted much attention. However, efficacy and safety of TSO therapy are still not well described. The aim of the study was to perform a meta-analysis to assess the effectiveness of TSO therapy in IBD.
Methods PubMed, Embase, Web of Science, ClinicalTrials.gov, and Cochrane Library were searched from inception to August 2017. Only randomized, double-blind, placebo-controlled trials (RCTs) were included. The pooled estimate rates were performed by meta-analysis and reported according to the standard Cochrane guidelines and the PRISMA statement.
Results In ulcerative colitis study (3 RCTs, n = 74), the induced rates of clinical remission and clinical response were 10.8% (4/37) and 53.8% (21/39) in TSO group, while 6.7% (2/30) and 29.0% (9/31) in placebo group (all P > .26). Twenty-two (9/41) percent of patients in TSO group experienced at least 1 adverse event compared with 27.3% (9/33) of placebo [relative ratio (RR) 0.75, 95% confidence interval (95% CI) 0.17-3.27]. In Crohn disease study (3 RCTs, n = 538), 40.7% (74/182) of patients in TSO group achieved clinical remission compared with 42.9% (90/210) of placebo (RR 0.95, 95% CI 0.75-1.20); 45.9% (141/307) of patients in TSO group entered clinical response compared with 45.1% (151/335) of placebo (RR 1.02, 95% CI 0.86-1.21). There were sparse data of adverse events reporting both TSO and placebo group (RR 1.00, 95% CI 0.88-1.13).
Conclusion TSO therapy showed no statistical benefit for IBD patients, so it suggested clinicians consider its value carefully before putting into clinical practice. Perhaps continued investigations of larger sample size are necessary due to the previous results with lack of power.
Izvorni podaci
- DOI
- 10.1097/md.0000000000012087
- PMID
- 30142867
- PMCID
- PMC6113037
- Provjereno
- 2026-07-26
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